Wikidata

(Q28141107)

English

New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome

scientific article (publication date: 12 October 2000)

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Statements

title
New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome (English)
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author name string
T C Cox
series ordinal
1
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L R Allen
series ordinal
2
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L L Cox
series ordinal
3
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B Hopwood
series ordinal
4
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B Goodwin
series ordinal
5
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E Haan
series ordinal
6
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G K Suthers
series ordinal
7
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publication date
12 October 2000
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volume
9
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issue
17
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page(s)
2553-62
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Identifiers

DOI
10.1093/HMG/9.17.2553
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